Evidence map›Paper›PMID 31915413›Full record

ArticleSarcoma2019

Prognostic Factors in Dedifferentiated Chondrosarcoma: A Retrospective Analysis of a Large Series Treated at a Single Institution.

Ruoyu Miao, Edwin Choy, Kevin A Raskin, Joseph H Schwab, Gunnlaugur Petur Nielsen, Vikram Deshpande, Ivan Chebib, Thomas F DeLaney, Francis J Hornicek, Gregory M Cote and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Sarcoma, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Ruoyu MiaoDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID https://orcid.org/0000-0003-4286-5742
Edwin ChoyDepartment of Medical Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID https://orcid.org/0000-0001-9896-8084
Kevin A RaskinHarvard Medical School, Boston, MA 02115, USA.
Joseph H SchwabHarvard Medical School, Boston, MA 02115, USA.
Gunnlaugur Petur NielsenHarvard Medical School, Boston, MA 02115, USA.
Vikram DeshpandeHarvard Medical School, Boston, MA 02115, USA.
Ivan ChebibHarvard Medical School, Boston, MA 02115, USA.ORCID https://orcid.org/0000-0002-6826-0226
Thomas F DeLaneyDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID https://orcid.org/0000-0002-0346-3487
Francis J HornicekHarvard Medical School, Boston, MA 02115, USA.
Gregory M CoteDepartment of Medical Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID https://orcid.org/0000-0003-0181-886X
Yen-Lin E ChenDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID https://orcid.org/0000-0002-8556-2349
Harvard University · USMassachusetts General Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDedifferentiated chondrosarcomas (DDCSs) are highly malignant tumors with a dismal prognosis and present a significant challenge in clinical management.

methodsIn an IRB approved retrospective protocol, we identified 72 patients with DDCS treated at our institution between 1993 and 2017 and reviewed clinicopathological characteristics, treatment modalities, and outcomes to analyze prognostic factors.

resultsFemur (44.4%), pelvis (22.2%), and humerus (12.5%) were most commonly involved sites. Twenty-three patients (31.9%) presented with distant metastasis, and 3 (4.2%) of them also had regional lymph node involvement. The median overall survival (OS) was 13.9 months. On multivariate analysis, pathological fracture, larger tumor size, lymph node involvement, metastasis at diagnosis, extraosseous extension, and undifferentiated pleomorphic sarcoma component correlated with worse OS, whereas surgical resection and chemotherapy were associated with improved OS. For progression-free survival (PFS), pathological fracture and metastasis at diagnosis showed increased risk, while chemotherapy was associated with decreased risk. Among patients who received chemotherapy, doxorubicin and cisplatin were significantly associated with improved PFS but not OS. Among patients without metastasis at diagnosis, 17 (34.7%) developed local recurrence. Thirty-one (63.3%) developed distant metastases at a median interval of 18.1 months. On multivariate analysis, R1/R2 resection was related with local recurrence, while macroscopic dedifferentiated component was associated with distant metastasis.

conclusionsThe prognosis of DDCS is poor. Complete resection remains a significant prognostic factor for local control. Chemotherapy with doxorubicin and cisplatin seems to have better PFS. More prognostic, multicenter trials are warranted to further explore the effectiveness of chemotherapy in selected DDCS patients.

Identifiers

PMID31915413
PMCPMC6930709
OpenAlexW2995321119

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.